Dr. Susan Roseanne Panny M.D.
Pediatrician
201 W Preston St Suite 424 Baltimore MD, 21201About
Dr. Susan Panny is a pediatrician practicing in Baltimore, MD. Dr. Panny is a doctor who specializes in the health care of children. As a pedicatrician, Dr. Panny diagnoses and treats infections, injuries, diseases and other disorders in children. Pediatricians typically work with infants, children, teenagers and young adults up to age 21. They practice medical care as well as preventative health care. Dr. Panny can oversee and manage the physical, mental and emotional health of their patients.
Education and Training
University of Maryland School of Medicine 1974
Board Certification
Medical GeneticsAmerican Board of Medical GeneticsABMG
PediatricsAmerican Board of PediatricsABP
Provider Details
Expert Publications
Data provided by the National Library of Medicine- US newborn screening system guidelines II: follow-up of children, diagnosis, management, and evaluation. Statement of the Council of Regional Networks for Genetic Services (CORN).
- A case-control study of nonsyndromic oral clefts in Maryland.
- Birth delivery mode modifies the associations between prenatal polychlorinated biphenyl (PCB) and polybrominated diphenyl ether (PBDE) and neonatal thyroid hormone levels.
- HIV antibody seroprevalence among childbearing women surveyed in Maryland.
- Deletions of proximal 15q and non-classical Prader-Willi syndrome phenotypes.
- Characteristics influencing informed consent on a congenital malformations registry.
- Inherited X-chromosome inverted tandem duplication in a male traced to a grandparental mitotic error.
- A complex rearrangement, including a deleted 8q, in a case of Langer-Giedion syndrome.
- A temperature sensitive mutation of the beta'-subunit of DNA-dependent RNA polymerase from E. coli T 16.
- Studies of deoxycytidylate deaminase from T4-infected Escherichia coli.
- Population heterogeneity of the Hpa I restriction site associated with the beta globin gene: implications for prenatal diagnosis.
- Duplication of chromosome 10p: confirmation of regional assignments of platelet-type phosphofructokinase.
- Prenatal diagnosis of sickle cell anemia by restriction and endonuclease analysis: HindIII polymorphisms in gamma-globin genes extend test applicability.
- Association study of transforming growth factor alpha (TGF alpha) TaqI polymorphism and oral clefts: indication of gene-environment interaction in a population-based sample of infants with birth defects.
- Chorionic villus sampling and transverse digital deficiencies: evidence for anatomic and gestational-age specificity of the digital deficiencies in two studies.
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